HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500525Generated: November 1, 2026
4-Bromophenacyl bromide → HCID 56962039, compound
https://huagongshe.com/reaction/1500525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | (4S)-1-(tert-Butoxycarbonyl)-4-methoxy-L-proline | HCID 15222286 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 56962039 | HCID 56962039 | 96.1% |
Reaction Steps
To a solution of (2S,4S)-4-methoxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (900 mg, 3.67 mmol), and p-bromophenacyl bromide (1.02 g, 3.67 mmol) in DCM (20 mL) under nitrogen, was added N,N-diisopropylethylamine (1.92 mL, 11.01 mmol). The resulting mixture was stirred at 35° C. for 3 h and concentrated under vacuum. The crude intermediate was dissolved in toluene (150 mL), ammonium acetate (5.66 g, 73.4 mmol) was added, and the resulting mixture was stirred at 95° C. overnight, cooled to RT, and washed with water (2×10 mL). The organic layer was dried over magnesium sulfate, filtered, concentrated and purified by silica gel chromatography (24 g, ethyl acetate/hexanes 0 to 60%) to give the title intermediate (1.49 g, 96% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206159B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-39f2ffc450a34c12b083a48bf925c29c |
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| Source note | uspto-grants-2015_12 |
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